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Inducing Meningococcal Meningitis Serogroup C in Mice via Intracisternal Delivery
Published on: November 5, 2019
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Meningococcal vaccine antigen diversity in global databases
Carina Brehony1, Dorothea M Hill, Jay Lucidarme
1Department of Zoology, University of Oxford, South Parks Road, Oxford, United Kingdom.
Summary
Developing effective vaccines against serogroup B meningococcal disease requires analyzing protein variants. This study found that specific combinations of antigen variants in multicomponent vaccines show potential for long-term, widespread protection against meningococcal disease.
Area of Science:
- Microbiology
- Vaccinology
- Genomics
Background:
- The absence of a serogroup B meningococcal vaccine necessitates exploring alternative protein-based vaccine candidates.
- These proteins often exhibit antigenic variation, complicating vaccine development.
- Publicly accessible databases like Neisseria PubMLST and MRF-MGL aid in analyzing these variations.
Purpose of the Study:
- To investigate the prevalence of components in six proposed meningococcal vaccine formulations.
- To identify prevalent antigen variants and their associations with serogroups and genotypes.
- To assess the potential for long-term protection offered by different vaccine formulations.
Main Methods:
- Analysis of antigen-encoding gene variants using data from Neisseria PubMLST and MRF-MGL.
- Deduction of component prevalence in proposed meningococcal vaccine formulations.
- Statistical analysis of variant combinations and their associations with serogroups/genotypes.
Main Results:
- Despite high diversity, a limited number of antigenic variants for each vaccine antigen were prevalent.
- Strong associations were found between specific variant combinations, serogroups, and genotypes.
- Multicomponent/multivariant vaccines showed the highest levels of identical sequences globally and in the MRF-MGL.
- Certain antigen variant combinations demonstrated prevalence over decades across diverse locations.
Conclusions:
- Vaccine formulations with judiciously chosen antigen variants offer potential for long-term, geographically widespread protection against meningococcal disease.
- Multivariant formulations are particularly relevant during periods of low disease incidence.
- Continuous surveillance is essential to monitor evolving vaccine antigen prevalence.
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